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A novel compound heterozygous COL4A4 mutation in a Chinese family with Alport syndrome: A care case report.
Chen, Ji-Yu; Cui, Jing-Jing; Yang, Xi-Ran; Li, Yan-Fang; Zhang, Yan-Hua; Chen, Jia-Ni; Lin, Jun-Yu; Zhao, Bo.
Afiliação
  • Chen JY; Department of Nephrology & Rheumatology, Kunming Children's Hospital, Kunming, Yunnan, China.
  • Cui JJ; Department of Nephrology & Rheumatology, Kunming Children's Hospital, Kunming, Yunnan, China.
  • Yang XR; Department of Nephrology & Rheumatology, Kunming Children's Hospital, Kunming, Yunnan, China.
  • Li YF; Department of Nephrology & Rheumatology, Kunming Children's Hospital, Kunming, Yunnan, China.
  • Zhang YH; Department of Nephrology & Rheumatology, Kunming Children's Hospital, Kunming, Yunnan, China.
  • Chen JN; Dali University, Dali, Yunnan, China.
  • Lin JY; Dali University, Dali, Yunnan, China.
  • Zhao B; Department of Nephrology & Rheumatology, Kunming Children's Hospital, Kunming, Yunnan, China.
Medicine (Baltimore) ; 100(47): e27890, 2021 Nov 24.
Article em En | MEDLINE | ID: mdl-34964757
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Colágeno Tipo IV / Nefrite Hereditária Limite: Child / Humans / Male País como assunto: Asia Idioma: En Ano de publicação: 2021 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Colágeno Tipo IV / Nefrite Hereditária Limite: Child / Humans / Male País como assunto: Asia Idioma: En Ano de publicação: 2021 Tipo de documento: Article